310:肠道菌群介导的新型口服给药系统

Parmandeep Kaur, D. Choudhury
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引用次数: 0

摘要

口服给药是最方便的给药途径,近80%的药物通过口服给药。尽管口服给药具有自我给药、方便、经济、无痛、无创等优点,但由于药物通过胃肠道的渗透性低,仅吸收给药剂量的3-10%,生物利用度降低,因此口服给药是一个主要挑战。因此,由于药物在胃和小肠内的半衰期有限(~30分钟),为了达到有效反应,过量的药物需要通过口服途径给药,这导致了许多副作用,包括肠易激综合征、痔疮、胃肠道溃疡以及癌症、肠炎、溃疡性结肠炎等。此外,未代谢的药物混合到土壤和饮用水等环境中会导致生物放大,并推断微生物中抗生素耐药性的发展。因此,增加胃肠道的半衰期将是解决这个问题的一个很好的办法。在这项工作中,我们展示了使用表面封装的介孔(2-3 nm)碳水化合物纳米颗粒(大小为15-25 nm)在代谢活跃的罗伊氏乳杆菌(一种GRAS细菌)上作为适合口服给药的药物载体。我们进一步证明了使用细菌介导的药物传递系统来增强5-氟尿嘧啶对肉瘤-180癌的效力。细菌表面包被的纳米颗粒的载药量为其干重的12-15%。颗粒在模拟胃液和肠液中也表现出长达48小时的优异稳定性。此外,颗粒显示药物的持续释放长达16小时,其中在30分钟-1小时之间的初始爆炸(释放高达30%)后,药物的稳定释放长达6.5至7小时,其中95%的药物在该窗口内被释放。临床前研究表明,经口服给药后,载药表面包封的微生物在小鼠的肠道肺泡区有固支作用。此外,一项使用小鼠Sarcoma-180肿瘤模型的研究显示,在10天的治疗过程中,最佳剂量为50 mg/Kg时,寿命延长,肉瘤-180实体瘤体积缩小(高达-95%),而对照组只有~75%。使用微生物载体,在次优剂量(25 mg/kg)下也观察到肿瘤体积减少高达75%。从血液参数分析和组织学分析来看,肝和肾病毒性的降低也很明显,使用这种给药工具也很突出。这种新颖的设计和发展使该系统非常适合用于低溶解度或低渗透性的口服给药药物。引文格式:Parmandeep Kaur, Diptiman Choudhury。肠道菌群介导的新型口服给药系统[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第310期。
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Abstract 310: Gut microflora mediated novel oral drug delivery system
The oral route is the most convenient route of drug administration and almost 80 % of the drugs are administered through this route. Despite many advantages like self-administrable, convenient, economic, pain-free, non-invasive, etc, the oral route is a major challenge for drugs which has low permeability through the GI tract leading to absorption of only 3-10% of the administered dose and reduced bioavailability. Therefore, due to limited half-life (~30 mins) in the stomach and small intestine, to achieve effective response excess of drugs need to be administrated through an oral route which causes many side effects including irritable bowel syndrome, hemorrhoids, gastrointestinal ulcers, and cancer, Cohn9s disease, ulcerative colitis, etc. Besides mixing of the un-metabolized drug to the environment like soil and drinking water causes bio-magnifications and infer the development of antibiotic resistance in microorganisms. Therefore, an increase of half-life in the GI tract would be a great solution to solve this problem. Here in this work, we show the use of surface encapsulated mesoporous (2-3 nm) carbohydrate nanoparticles of (15-25 nm in size) on metabolically active Lactobacillus reuteri, a GRAS bacterium, as a drug carrier vehicle suitable for oral administration. We have further demonstrated the use of bacteria mediated drug delivery system for enhancing the potency of 5-fluorouracil against Sarcoma-180 cancer. The bacterial surface encapsulated nanoparticles particles showed 12-15% drug loading capacity of its dry weight. The particles also showed excellent stability up to 48 h in simulated gastric and intestinal fluid. Further, the particles showed sustained release of the drug for up to 16 h, where after an initial blast (release up to 30 %) between 30 min-1 h a steady release of drug was obtained for up to 6.5 to 7 h, where 95% of the drug got released within that window. The pre-clinical study showed anchorage of drug-loaded surface encapsulated microbes to the mice intestinal alveolar regions after feeding through the oral route. Further, a study using murine Sarcoma-180 tumor model showed enhancement of life span and enhanced shrinkage of the Sarcoma-180 solid tumor volume (up to -95%) at optimal dose 50 mg/Kg dose, in comparison with control only ~75% throughout 10 days9 treatment. Up to 75 % reduction of tumor volume was also observed in suboptimal dose (25 mg/kg) using the microbial vehicle. Reduction of hepatic and nephrotic toxicity was also evident from the blood parameters analysis and histological analysis was also prominent using this delivery tool. This novel design and development make this system ideal for use in orally administrable drug shaving low solubility or permeability or both. Citation Format: Parmandeep Kaur, Diptiman Choudhury. Gut microflora mediated novel oral drug delivery system [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 310.
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